For one of our clients, a global manufacturing company specialized in the life sciences sector, we are looking for a Manufacturing Scientist based in the canton of Fribourg. Your Impact:Implement and optimize robust, compliant, and high-performing manufacturing processes aligned with quality strategyCapitalize on and share your expertise throughout the entire product lifecycleDraft, review, and approve key technical documents (batch records, procedures,
For one of our clients, a global manufacturing company specialized in the life sciences sector, we are looking for a Manufacturing Scientist based in the canton of Fribourg. Your Impact:Implement and optimize robust, compliant, and high-performing manufacturing processes aligned with quality strategyCapitalize on and share your expertise throughout the entire product lifecycleDraft, review, and approve key technical documents (batch records, procedures,
Strategic Business Development & In-Licensing Specialist - 100%Starting date : ASAP Location : GenevaType of role : Permanent role Your ResponsibilitiesGenerate high-level scientific and commercial intelligence on potential licensors and therapeutic target areas.Manage business intelligence tools and databases (e.g., IMS, Evaluate Pharma) to support data-driven decision-making.Actively source, evaluate, and execute prioritized in-licensing
Strategic Business Development & In-Licensing Specialist - 100%Starting date : ASAP Location : GenevaType of role : Permanent role Your ResponsibilitiesGenerate high-level scientific and commercial intelligence on potential licensors and therapeutic target areas.Manage business intelligence tools and databases (e.g., IMS, Evaluate Pharma) to support data-driven decision-making.Actively source, evaluate, and execute prioritized in-licensing
About the roleWe’re looking for a CQV Engineer to drive the validation of equipment, systems, and facilities in a regulated pharmaceutical environment. You will coordinate installations, author and execute IQ/OQ/PQ protocols, and document results in compliance with cGMP/GxP requirements—ensuring our operations are safe, compliant, and inspection-ready.What you’ll doPlan and coordinate CQV activities for facilities & utilities (e.g., HVAC, cleanrooms, WFI,
About the roleWe’re looking for a CQV Engineer to drive the validation of equipment, systems, and facilities in a regulated pharmaceutical environment. You will coordinate installations, author and execute IQ/OQ/PQ protocols, and document results in compliance with cGMP/GxP requirements—ensuring our operations are safe, compliant, and inspection-ready.What you’ll doPlan and coordinate CQV activities for facilities & utilities (e.g., HVAC, cleanrooms, WFI,
For our client, a dynamic international biotechnology company focused on clinical-stage development, and currently expanding their global portfolio and accelerating growth outside of China, we recruit a:(Senior/Executive Director) Head of Business Development, Ex-China Location: Based in Basel, Switzerland / Remote modelResponsabilities:As the Head of Ex-China Business Development, you will be pivotal in orchestrating our client’s global expansion,
For our client, a dynamic international biotechnology company focused on clinical-stage development, and currently expanding their global portfolio and accelerating growth outside of China, we recruit a:(Senior/Executive Director) Head of Business Development, Ex-China Location: Based in Basel, Switzerland / Remote modelResponsabilities:As the Head of Ex-China Business Development, you will be pivotal in orchestrating our client’s global expansion,
For one of our clients, a world leader in in-vitro diagnostics, we are currently looking for a System Integration Engineer.General Information:Start date: 01.04.2026Latest Start Date: 01.06.2026Planned duration: 1 year with the possibility of extensionWorkplace: RotkreuzWorkload: 80-100%Home Office: predominantly on-site, occasional home office work possible for documentationTeam: 15 peopleDepartment: SSD - CHU & CB Integration & Testing (DSRCSE)Working
For one of our clients, a world leader in in-vitro diagnostics, we are currently looking for a System Integration Engineer.General Information:Start date: 01.04.2026Latest Start Date: 01.06.2026Planned duration: 1 year with the possibility of extensionWorkplace: RotkreuzWorkload: 80-100%Home Office: predominantly on-site, occasional home office work possible for documentationTeam: 15 peopleDepartment: SSD - CHU & CB Integration & Testing (DSRCSE)Working
Role OverviewWe are seeking an experienced Privileged Access Management (PAM) Subject Matter Expert (SME) to lead the design, implementation, and operational maturity of PAM capabilities across a complex enterprise environment.This role is responsible for establishing and enforcing robust security controls for privileged identities, ensuring compliance with regulatory and security standards, and embedding PAM as a core enterprise security capability.The
Role OverviewWe are seeking an experienced Privileged Access Management (PAM) Subject Matter Expert (SME) to lead the design, implementation, and operational maturity of PAM capabilities across a complex enterprise environment.This role is responsible for establishing and enforcing robust security controls for privileged identities, ensuring compliance with regulatory and security standards, and embedding PAM as a core enterprise security capability.The
Location: Bulle, SwitzerlandActivity rate : 100%Type of contract: Temporary contractStart Date: ASAPEnd Date: 30.09.2026 (with a possible extension) We are looking for a dedicated MSAT Bio DS Process Specialist to be based in our manufacturing site in Bulle, Switzerland.As an MSAT Bio DS Process Specialist, you will play a pivotal role in the development and optimization of downstream processes for biologics. Your responsibilities will include ensuring
Location: Bulle, SwitzerlandActivity rate : 100%Type of contract: Temporary contractStart Date: ASAPEnd Date: 30.09.2026 (with a possible extension) We are looking for a dedicated MSAT Bio DS Process Specialist to be based in our manufacturing site in Bulle, Switzerland.As an MSAT Bio DS Process Specialist, you will play a pivotal role in the development and optimization of downstream processes for biologics. Your responsibilities will include ensuring
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